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Effects of Simvastatin and Cholestyramine in Familial and Nonfamilial Hypercholesterolemia
Evan Stein, MD, PhD;
Robert Kreisberg, MD;
Valery Miller, MD;
Geraldine Mantell, MD;
Linda Washington, RN;
Deborah R. Shapiro, DrPH
Arch Intern Med. 1990;150(2):341-345.
Abstract
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Simvastatin, a potent inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, was compared with cholestyramine resin in a randomized open-label 12-week multicenter study of 251 high-risk patients with familial or nonfamilial hypercholesterolemia. Simvastatin, 20 mg and 40 mg daily, produced mean reductions in total cholesterol of 26% and 33%, respectively, and reductions in low-density lipoprotein cholesterol level of 32% and 40%. Cholestyramine resin, 4 to 12 g twice daily, reduced total cholesterol and low-density lipoprotein cholesterol levels 15% and 21%, respectively. High-density lipoprotein cholesterol levels were increased 8% to 10% by all treatments. Plasma triglyceride levels were moderately decreased by simvastatin treatment, while triglyceride levels increased with cholestyramine treatment. Simvastatin was better tolerated than cholestyramine, which had numerous gastrointestinal tract side effects. No patient had a serious drug-related adverse event.
(Arch Intern Med. 1990;150:341-345)
Author Affiliations
From Christ Hospital Cardiovascular Research Center, Cincinnati, Ohio (Dr Stein); University of Alabama, Mobile, Ala (Dr Kreisberg); George Washington University Lipid Research Clinic, Washington, DC (Dr Miller); and Merck Sharp & Dohme Research Laboratories, West Point, Pa (Drs Mantell and Shapiro and Ms Washington).
Footnotes
Accepted for publication September 1,1989.
Reprint requests to Christ Hospital Cardiovascular Center, 2350 Auburn Ave, Cincinnati, OH 45219 (Dr Stein).
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